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二硫化钼-超交联聚合物复合材料作为吸附剂用于高效液相色谱-荧光检测法测定环境水中的多环芳烃。

Molybdenum disulfide-hypercrosslinked polymer composite as an adsorbent for determination of polycyclic aromatic hydrocarbons in environmental water coupled with HPLC-FLD.

机构信息

Key Laboratory of Medicinal Chemistry and Molecular Diagnosis, Ministry of Education & College of Public Health, Hebei University, Baoding, 071002, China.

Key Laboratory of Analytical Science and Technology of Hebei Province, College of Chemistry and Environmental Science, Hebei University, Baoding, 071002, China.

出版信息

Mikrochim Acta. 2020 Mar 23;187(4):242. doi: 10.1007/s00604-020-4220-0.

Abstract

A composite was synthesized from two-dimensional molybdenum disulfide (MoS) nanosheets and hypercrosslinked polymers (HCP), and the composite was characterized by infrared spectroscopy, scanning electron microscopy, and specific surface area. The fluffy and porous structure and multiple adsorption sites (π-interaction, static electricity, hydrogen bonding) make it ideal for use as an adsorbent. A pipette tip solid-phase extraction with the composite as the adsorbent combined with HPLC-FLD was developed to determine trace amounts of polycyclic aromatic hydrocarbons (phenanthrene, anthracene, fluoranthene, pyrene, benzo(α)anthracene) in environmental water. Under optimal extraction conditions, the method has a wide linear range (0.5-100 ng mL) and low limit of detection (0.024-0.099 ng mL), and the recoveries of PAHs from spiked environmental water were 73.8% to 123.6% (relative standard deviation ≤ 6.7%, n = 3). Graphical abstract Schematic representation of a three-dimensional molybdenum disulfide-ethylenediamine-hypercrosslinked polymer composite (MoS-EDA-HCP) using pipette tip solid-phase extraction adsorbent for extracting trace levels of polycyclic aromatic hydrocarbons (PAHs) prior to HPLC-FLD. HCP, hypercrosslinked polymer; MoS, molybdenum disulfide; EDA, ethylenediamine.

摘要

采用二维二硫化钼(MoS)纳米片和超交联聚合物(HCP)合成了一种复合材料,并通过红外光谱、扫描电子显微镜和比表面积对其进行了表征。蓬松多孔的结构和多个吸附位点(π相互作用、静电力、氢键)使其成为理想的吸附剂。采用复合吸附剂的微量进样固相萃取与高效液相色谱-荧光检测法相结合,测定了环境水样中痕量多环芳烃(菲、蒽、荧蒽、芘、苯并(α)蒽)。在最佳萃取条件下,该方法具有较宽的线性范围(0.5-100ngmL)和较低的检测限(0.024-0.099ngmL),环境水样中多环芳烃的加标回收率为 73.8%至 123.6%(相对标准偏差≤6.7%,n=3)。

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